ENST00000265838.9:c.1250G>T
MANE Select
|
ENSP00000265838.4:p.Gly417Val
|
|
ENST00000671707.1:n.1345G>T
|
|
|
ENST00000672031.1:c.*237G>T
|
ENSP00000500463.1:n.*237G>T
|
|
ENST00000672284.1:c.980G>T
|
ENSP00000500444.1:p.Gly327Val
|
|
ENST00000672354.1:c.1271G>T
|
ENSP00000500490.1:p.Gly424Val
|
|
ENST00000672367.1:c.887G>T
|
ENSP00000500209.1:p.Gly296Val
|
|
ENST00000672580.1:c.*505G>T
|
ENSP00000500366.1:n.*505G>T
|
|
ENST00000672907.1:c.935G>T
|
ENSP00000500928.1:p.Gly312Val
|
|
ENST00000673000.1:n.1338G>T
|
|
|
ENST00000673531.1:c.980G>T
|
ENSP00000500163.1:p.Gly327Val
|
|
ENST00000265838.8:c.1250G>T
|
ENSP00000265838.4:p.Gly417Val
|
|
ENST00000533597.1:n.326G>T
|
|
|
NM_000019.3:c.1250G>T
|
NP_000010.1:p.Gly417Val
|
|
XM_006718834.2:c.980G>T
|
XP_006718897.1:p.Gly327Val
|
|
XM_006718835.2:c.980G>T
|
XP_006718898.1:p.Gly327Val
|
|
XM_006718835.3:c.980G>T
|
XP_006718898.1:p.Gly327Val
|
|
XM_017017681.1:c.980G>T
|
XP_016873170.1:p.Gly327Val
|
|
XM_017017682.2:c.872G>T
|
XP_016873171.1:p.Gly291Val
|
|
XM_017017683.2:c.872G>T
|
XP_016873172.1:p.Gly291Val
|
|
XM_024448511.1:c.980G>T
|
XP_024304279.1:p.Gly327Val
|
|
XM_024448512.1:c.980G>T
|
XP_024304280.1:p.Gly327Val
|
|
XM_024448513.1:c.980G>T
|
XP_024304281.1:p.Gly327Val
|
|
XM_024448514.1:c.980G>T
|
XP_024304282.1:p.Gly327Val
|
|
XM_024448515.1:c.980G>T
|
XP_024304283.1:p.Gly327Val
|
|
NM_000019.4:c.1250G>T
MANE Select
|
NP_000010.1:p.Gly417Val
|
|
NM_001386677.1:c.1271G>T
|
NP_001373606.1:p.Gly424Val
|
|
NM_001386678.1:c.935G>T
|
NP_001373607.1:p.Gly312Val
|
|
NM_001386679.1:c.953G>T
|
NP_001373608.1:p.Gly318Val
|
|
NM_001386681.1:c.980G>T
|
NP_001373610.1:p.Gly327Val
|
|
NM_001386682.1:c.980G>T
|
NP_001373611.1:p.Gly327Val
|
|
NM_001386685.1:c.980G>T
|
NP_001373614.1:p.Gly327Val
|
|
NM_001386686.1:c.980G>T
|
NP_001373615.1:p.Gly327Val
|
|
NM_001386687.1:c.980G>T
|
NP_001373616.1:p.Gly327Val
|
|
NM_001386688.1:c.980G>T
|
NP_001373617.1:p.Gly327Val
|
|
NM_001386689.1:c.980G>T
|
NP_001373618.1:p.Gly327Val
|
|
NM_001386690.1:c.980G>T
|
NP_001373619.1:p.Gly327Val
|
|
NM_001386691.1:c.980G>T
|
NP_001373620.1:p.Gly327Val
|
|
NR_170162.1:n.1225G>T
|
|
|
NR_170163.1:n.1283G>T
|
|
|